Securement device having an integral strap and dressing

ABSTRACT

A securement device for securing a catheter includes a retainer, a strap, a first anchor pad and a second anchor pad, a gap separating an edge of the first anchor pad from an adjacent edge of the second anchor pad. The retainer can include a first base member secured to an upper surface of the first anchor pad, a second base member secured to an upper surface of the second anchor pad, and a body coupled to the first and second base members. The body can include a portion spanning the gap separating the first anchor pad from the second anchor pad. The portion of the body can include an open channel through an upper surface of the body, the open channel aligned with the gap. The body can further include a first securement mechanism and a second securement mechanism. The strap can be rotatably coupled to the body.

PRIORITY

This application is a continuation of U.S. patent application Ser. No.14/764,979, which is a U.S. national stage application of InternationalPatent Application No. PCT/US2014/020207, filed Mar. 4, 2014, claimingthe benefit of priority to U.S. Provisional Application No. 61/789,412,filed Mar. 15, 2013, each of which is incorporated by reference in itsentirety into this application.

BACKGROUND Field of the Invention

The present invention relates generally to techniques, systems, anddevices for securing a catheter, catheter extension set, and/or othermedical article on a patient.

Description of the Related Art

Medical patients are often in need of repetitious administering offluids or medications, or repetitious draining of fluids. It is verycommon in the medical industry to utilize medical tubing to providevarious liquids or solutions to a patient. For example, medical tubingsuch as a catheter is often used to introduce fluids and medicationsdirectly into the patient or to withdraw fluids from the patient. Inmany cases, the catheter remains in place for many days. In someinstances, a catheter may be attached to a patient for an even lengthierperiod of time, and may require minimal movement for proper functioning.

It is often advantageous to restrict the movement of the catheter. Amoving catheter may cause discomfort to the patient, restrict theadministering of fluids or medications or the draining of fluids, causeinfection, or become dislodged from the patient unintentionally. Inorder to keep the catheter or other medical tubing properly positionedfor the duration of treatment, the catheter or medical tubing can bestabilized on the patient in a variety of ways. Most commonly, themedical provider may attempt to restrict movement of the catheter bysecuring the distal end of the catheter, or a portion of a medicaldevice connected to the catheter such as a connector fitting, to thepatient using tape. Medical providers commonly place long pieces of tapeacross the distal end of the catheter, often in a crisscross pattern, tosecure the catheter distal end to the patient. This securement isintended to inhibit disconnection between the catheter and the patientor between the catheter and another medical article, such as a drainagetube, as well as to prevent the catheter from catching on other objects,such as on a bed rail.

Stabilizing a catheter with tape upon the patient, however, has certaindrawbacks. For example, taped connections often collect contaminants anddirt. This potentially can lead to infection of the patient,particularly at an insertion site where the catheter is inserted intothe patient. Taped stabilization typically leaves the insertion siteexposed to these contaminants and dirt and other foreign objects thatmay be harmful to the patient and/or compromise the stabilization of thecatheter. Gathering or collecting of contaminants by the tape mayexacerbate any problems at the insertion site. Normal protocol thereforerequires periodic tape changes in order to inhibit germ growth. Suchperiodic changes, however, often disrupt any attempts or mechanisms usedto shield or protect the insertion site, and may compel detrimentalmanipulation of the areas around the insertion site. Furthermore, it maybe desirable to keep the insertion site of the medical article dryand/or otherwise protected from the external environment in order toreduce infections in and around the insertion site.

BRIEF DESCRIPTION OF DRAWINGS

The above mentioned and other features of the invention will now bedescribed with reference to the drawings of several embodiments of thepresent stabilization system. The illustrated embodiments of thestabilization system are intended to illustrate, but not to limit theinvention. The drawings contain the following figures:

FIG. 1 is a perspective view of an embodiment of a securement devicehaving an integral strap and dressing.

FIG. 2 is a top view of the securement device of FIG. 1.

FIG. 3A is a cross-sectional view of the securement device of FIG. 2taken along the line 3A-3C according to one embodiment.

FIG. 3B is a cross-sectional view of the securement device of FIG. 2taken along the line 3A-3C according to another embodiment.

FIG. 3C is a cross-sectional view of the securement device of FIG. 2taken along the line 3A-3C according to another embodiment.

FIG. 4 is a front view taken from the proximal end of the securementdevice of FIG. 1.

FIG. 5 is a rear view taken from the distal end of the securement deviceof FIG. 1.

FIG. 6 is another perspective view of the securement device of FIG. 1and shows a medical article positioned above the device.

FIG. 7 is another perspective view of the securement device of FIG. 1and shows a medical article placed in the open retainer.

FIG. 8 is a top view of the securement device of FIG. 1 secured to apatient with the dressing folded against the patient with the retainerin the closed position.

FIG. 9 is a cross-sectional view taken along the line 9-9 of thesecurement device of FIG. 8 with the medical article placed in theclosed retainer.

FIG. 9A is a partial top view of the securement device of FIG. 8 withthe strap removed.

FIG. 10 is a perspective view of a medical article.

FIG. 11 is an exploded view of the medical article of FIG. 10.

FIG. 12 is another perspective view of the medical article of FIG. 10.

FIG. 13 is a perspective view of the medical article of FIG. 10 beingused with a patient.

FIG. 14 is another perspective view of the medical article of FIG. 10being used with a patient.

FIG. 15 is another perspective view of the medical article of FIG. 10being used with a patient.

FIG. 16 is a perspective view of another embodiment of a securementdevice having an integral strap and dressing.

FIG. 17 is a top view of the securement device of FIG. 16 secured to apatient with the dressing folded against the patient with the retainerin the closed position.

DETAILED DESCRIPTION OF CERTAIN EMBODIMENTS

The following description and examples illustrate preferred embodimentsof the present securement device disclosed in the context of use withexemplary catheters. More specifically, the embodiments relate to astabilization device and related techniques that stabilize a medicalarticle in position on a patient. The embodiments of the securementdevice are illustrated with a catheter in use as part of a peripheralintravenous (“I.V.”) line.

It will be understood by those of skill in the art in view of thepresent disclosure that the securement device described can be used withother types of medical articles, including, but not limited to cathetersand catheter hubs of various design, either with or without connectorsor extension sets, such as central venous catheters, peripherallyinserted central catheters, hemodialysis catheters, Foley catheters, aswell as other designs of catheter hubs and catheter adaptors. Othermedical articles may include surgical drainage tubes, feeding tubes,chest tubes, nasogastric tubes, rectal drains, external ventriculardrains, chest tubes; any other sort of fluid supply or medical lines,connector fittings, and scopes, as well as electrical wires or cablesconnected to external or implanted electronic devices or sensors. Themedical articles can be a single medical article or a combination ofmedical articles.

The securement device described herein is especially adapted to arrestat least transverse movement of a catheter, as well as to hold medicalarticles against the patient and protect an area in proximity to aninsertion site. The securement device accomplishes this withoutmeaningfully impairing (i.e., substantially occluding) fluid flowthrough a lumen of the medical article or impairing insertion of themedical article. In some embodiments, retention mechanisms to accomplishthis include a channel, a strap that is securable about a medicalarticle, and an integrated dressing. In other embodiments, retentionmechanisms to accomplish this include a retention mechanism having acatheter hub, retainer having a channel shaped to receive the hub, andan integrated strap and dressing. The securement device may also preventmovement in a distal and/or proximate direction with respect to thelongitudinal axis. In some embodiments, retention mechanisms toaccomplish this include a retainer having at least one abutment.

Some embodiments of the securement device releasably engage a catheterhub. An extension set or other medical article can then be attached tothe secured catheter hub. This allows the extension set to bedisconnected from the securement device, and from the patient, for anyof a variety of known purposes, while leaving the catheter secured tothe patient. For instance, the medical provider may want to remove theextension set to clean or replace the extension set or to clean an areasurrounding where the extension set is located on the patient. Thedisengagement of the extension set from the securement device, however,can be accomplished without removing an anchor pad, dressing, and/orreleasing a retention mechanism. Thus, the medical provider may move theextension set without irritating the skin of the patient or disrupting acatheter (for instance, a cannula) inserted in the skin of the patient.

With reference now to FIG. 1, an embodiment of a securement device 100includes anchor pads 110 a and 100 b, base members 130 a and 130 b, adressing 120, and a retainer 200. The anchor pad 110 is configured to besecured to a patient's skin. The base members 130 a and 103 b areattached to an upper surface of the anchor pads 110 a and 100 b andconfigured to support the retainer 200. The retainer 200 is configuredto engage a medical article, for example a catheter or catheter hub, aswill be described in additional detail below.

To assist in the description of the components of embodiments of thesecurement device, the following coordinate terms are used, consistentwith the coordinate axes illustrated in FIG. 1. A “longitudinal axis” isgenerally parallel to a channel formed by anchor pads 110 a and 110 band spanned by the retainer 200. A “lateral axis” is normal to thelongitudinal axis and is generally parallel to the plane of the retainer200. A “transverse axis” extends normal to both the longitudinal andlateral axes. In addition, as used herein, “the longitudinal direction”refers to a direction substantially parallel to the longitudinal axis;“the lateral direction” refers to a direction substantially parallel tothe lateral axis; and “the transverse direction” refers to a directionsubstantially parallel to the transverse axis. The terms “proximal” and“distal” are used in reference to the center of the patient's body, aswill be understood by one of skill in the art.

As can be seen in FIG. 1, the anchor pads 110 a and 110 b are positionedroughly parallel to each other and spaced apart by a gap 111. The gap111 can form a channel along the longitudinal axis for receiving amedical article such as a catheter. As will be described in greaterdetail below, the anchor pads 110 a and 110 b of the embodiment shown inFIG. 1 are shaped for use on a hand of a patient. However, other shapesand configurations of anchor pads 110 a and 110 b are possible andwithin the scope of this disclosure. In some embodiments, one anchor padis used.

The anchor pads 110 a and 110 b have a lower adhesive surface (notshown) which may adhere to the skin of a patient and an upper layer. Theupper layer of the anchor pads 110 a and 110 b is configured to supportat least the retainer 200. In some embodiments, the upper layer isconfigured to support at least the base members 130 a and 130 b. Incombination, the lower adhesive surface, upper layer, and possibly oneor more intermediate layers may comprise a laminate structure. Asuitable laminate that comprises a foam or woven material with anadhesive layer is available commercially from Avery Dennison ofPainsville, Ohio. The anchor pads 110 a and 110 b may be configured as aflexible structure configured to conform to the surface of a patient'sskin.

The lower adhesive surface or layer may be a medical-grade adhesive andcan be either diaphoretic or nondiaphoretic, depending upon theparticular application. The lower adhesive surface may have additionaltypes of medical adhesives laminated thereto. In some embodiments, thelower adhesive layer comprises an anti-bacterial or anti-microbialmaterial. For example, the lower adhesive layer may comprise one or moreoligodynamic metal salts or oxides, or a combination of salts andoxides. In some embodiments, the lower adhesive layer comprises a silvermaterial, for example a silver salt, colloid, or complex. The adhesivesurface may be a solid layer or may be configured as an intermittentlayer such as in a pattern of spots or strips. The lower adhesivesurface can be applied to the anchor pads 110 a and 110 b duringmanufacture, and may be further covered with a release liner asdescribed below. Alternatively, it is possible to apply a double-sidedadhesive tape to the upper layer before application.

The upper layer of the anchor pads 110 a and 100 b may comprise a foam(e.g., closed-cell polyethylene foam) or woven material (e.g., tricot)layer. A surface of the foam or woven material layer constitutes theupper layer of the anchor pads 110 a and 110 b. In the alternative, theupper layer may comprise an upper paper or other nonwoven cloth layer,and an inner foam layer may be placed between the upper layer and loweradhesive surface.

As shown, the anchor pads 110 a and 110 b include removable releaseliners 115 a and 115 b on a lower surface of the anchor pads 110 a and110 b. The removable release liners 115 a and 115 b may cover the loweradhesive surface before use. The release liners may resist tearing andbe divided into a plurality of pieces to assist removal of the releaseliners and ease attachment of the anchor pads 110 a and 110 b to apatient's skin. The release liners may be divided into two adjacentpieces. The liners may be made of a paper, plastic, polyester, orsimilar material. For example, the release liners 115 a and 115 b maycomprise a material made of polycoated, siliconized paper, or anothersuitable material such as high density polyethylene, polypropylene,polyolefin, or silicon coated paper. As illustrated in FIG. 1, therelease liners 115 a and 115 b include tabs that extend beyond the edgeof the anchor pads 110 a and 110 b to allow a medical provider to easilygrip the release liners 115 a and 115 b and remove them from the anchorpads 110 a and 110 b. The tabs may be located at any edge of the anchorpads 110 a and 110 b and may be any suitable size or shape.

With reference now to the dressing 120, it can be seen in FIG. 1 thatthe dressing 120 is attached to and/or integrated with anchor pad 110 a.The dressing 120 is configured to fold, bend, or rotate down over theinsertion site area 116 defined by the area in between the anchor pads110 a and 110 b and proximal to the retainer 200. A proximal extendedportion of the anchor pad 110 a can provide an attachment area to attachor integrate the dressing 120 with the anchor pad 110 a. Additionally,the extended portion may longitudinally offset the dressing 120 from alocation where the retainer 200 is supported by the anchor pad 110 asuch that when the dressing 120 is folded down over the insertion site,the dressing 120 will not substantially cover or obstruct a catheter hubstabilized by the securement device 100 or the retainer 200 itself.

The dressing 120 and the anchor pad 110 a may be formed as an integral,single piece. Alternatively, the dressing 120 and the anchor pad 110 amay be formed separately and then attached together. In this case, thedressing 120 and the anchor pad 110 a may be attached by any means ormechanism that allows the dressing 120 to fold, bend, or rotate downover the insertion site area. Attachment means include glue or adhesive,a weld of the materials, heat sealing, mechanical fasteners such asstaples or eyelets, or other such means of attachment. The anchor pad110 a may be configured in any shape and size that allows attachment orintegration of the dressing 120 with the anchor pad 110 a. The dressing120 may be attached to an upper surface of the anchor pad 110 a, forexample within an outer circumference of the anchor pad 110 a. In theillustrated embodiment, the dressing 120 is secured to an edge of theanchor pad 110 a that is generally parallel to a longitudinal axis. Thedressing 120, however, may be attached to or integrated with the anchorpad 110 a such that the dressing 120 is skewed with respect to alongitudinal and/or a lateral axis.

In some embodiments, the anchor pad 110 a, the dressing 120, and/or theattachment means described above are configured to allow selectivedisconnection of the dressing 120 from the anchor pad 110 a. Forexample, when the anchor pad 110 a and the dressing 120 are integrallyformed, the region in which the dressing pad 120 folds may be scouredsuch that a medical provider may tear the dressing 120 away from theanchor pad 110 a. Of course, other means of removal or release may beemployed to allow the dressing 120 to be disconnected from the anchorpad 110 a.

A release liner 121 may cover an adhesive surface 124 of the dressing120 and may also cover an occlusive layer 126 of the dressing 120, asshown in FIG. 1. The adhesive surface 124 is configured to adhere to theskin of a patient and/or to portions of the upper layer of the anchorpads 110 a and 110 b. The release liner 121 may cover the entire surfaceof the dressing 120 or may only cover adhesive portions of the dressing120. As illustrated in FIG. 1, the release liner 121 covers less thanthe entire surface of the dressing 120 and the edge 122 of the dressingis not covered by the release liner 121. In this way, the uncovered edge122 can function as a tab, allowing a medical provider to easily gripthe release liner and remove it from the dressing 120. In someembodiments, the release liner 121 extends past the edge of the dressingto form a tab. The tab may be located at any edge of the dressing 120,or a tab that projects out from the release liner 121 may be locatedwithin an area defined by the edges of the dressing 120. The releaseliner 121 may include an anti-microbial or anti-bacterial material orcoating, and/or have silver particles dispersed throughout. The dressing120 and release liner 121 may be prepared such that the release liner121 maintains a covered surface of the occlusive layer 126 in asterilized state. The release liner 121 may be configured similar to therelease liner covering the lower adhesive surface of the anchor pad 110,described above.

In the illustrated embodiment, the adhesive surface 124 is formed in aring shape on the periphery of the occlusive layer 126. This ringconfiguration will encircle the insertion site area when the adhesivelayer 124 is adhered to the skin of the patient, but will not adhere tothe point of insertion. Advantageously, this will reduce the likelihoodof aggravating or excoriating the insertion site or skin around theinsertion site, and will reduce the likelihood of introducingcontaminants and/or liquid near or into the point of insertion. Inaddition, the adhesive surface 124 will not contact the catheter 610 orcatheter hub 630 when the adhesive surface 124 is adhered to the skin.The ring is broken at a notch or indent 128 in the occlusive layer 126to allow a catheter and/or catheter hub to be covered without beingcontacted by the adhesive surface 124. Thus, the adhesive surface willnot adhere or stick to the catheter and/or the catheter hub. In thisway, sticky residues and buildup on the catheter and catheter hub may bereduced or avoided.

The adhesive surface 124 may instead cover all or a majority of theocclusive layer 126. Such configuration will increase the contact areaof the adhesive surface 124 with the skin of the patient and withportions of the anchor pads 110 a and 110 b, and may result in a moresecure attachment of the dressing 120 to the patient. The adhesivesurface 124 may be configured similar to the lower adhesive surface ofthe pads 110 a and 110 b, described above.

The occlusive layer 126 is configured to be waterproof or otherwiseimpermeable to liquids and in some embodiments also restricts the flowof air. In other embodiments, the occlusive layer 126 may be configuredto be breathable, allowing air and/or moisture near an insertion sitethrough to the other side of the occlusive layer 126 and away from theinsertion site, while keeping at least external moisture on the otherside of the occlusive layer 126 away from the insertion site. In someembodiments, the occlusive layer 126 is impermeable to viruses andbacteria, and may comprise or be coated with an anti-bacterial oranti-microbial material. In some embodiments, the occlusive layer 126comprises or is coated with a waxy material. In some embodiments, theocclusive layer 126 comprises a film which may or may not betransparent.

Selection of a transparent film or semi-transparent film for use as theocclusive layer 126 may allow a medical provider to see the insertionsite and any administered catheter. In this way, potential infections orinflammation may be visualized through the transparent film. In someembodiments, the occlusive layer 126 is absorbent. In some embodiments,the occlusive layer 126 comprises an absorbent acrylic, an alginate,foam, a hydrocolloid, and/or a hydrogel material, and/or may comprise asilver material, for example a silver salt, colloid, or complex. In oneembodiment, one or more oligodynamic metal salts or oxides, or acombination of salts and oxides are used in or on the occlusive layer126 as an antimicrobial agent. In some embodiments, the occlusive layer126 is configured similar to the upper layer of the anchor pads 110 aand 110 b.

As described above, the occlusive layer 126 comprises a notch orindentation 128. This notch may reduce stress on the dressing 120 whenthe dressing is applied over a catheter and/or catheter hub. Thedressing 120 may be configured to provide a waterproof seal around aninsertion site when applied to the skin of a patient over a catheterand/or catheter hub. In some embodiments, the dressing 120 is stillbreathable while the waterproof seal is created.

In some embodiments, the dressing 120 comprises a hemostatic dressing.In such embodiments, securing the dressing 120 over an insertion site orother wound may inhibit blood from flowing from the site. For example,the dressing 120 may comprise or be coated with a hemostatic orantihemorrhagic agent such as chitosan or other polysaccharide, acollagen like microfibrillar hemostat, anhydrous aluminum sulfate,potassium alum, titanium dioxide, a gelatin, or a solution of thrombin.

Continuing with FIG. 1, the base members 130 a and 130 b can have alower surface secured to the upper surface of the anchor pads 110 a and110 b and an upper surface secured to at least a portion of the lowersurface of the retainer 200. Although the base members 130 a and 130 bare shown as having a roughly rectangular shape with rounded ends, thebase members 130 a and 130 b may be shaped in any of a multitude ofways. The base members 130 a and 130 b can be formed with the same ordifferent materials as the retainer 200. In one embodiment, the basemembers 130 a and 130 b and the retainer 200 comprise a single, integralpiece. The base members 130 a and 130 b, anchor pads 110 a and 110 b,and retainer 200 may be secured together by any means or mechanismincluding glue or adhesive, a weld of the materials, heat sealing,mechanical fasteners such as staples or eyelets, or other such means ofattachment. In some embodiments, the base members 130 a and 130 b aresemi-rigid or flexible. In this way, the base members 130 a and 130 bcan provide a transition between the relatively pliable anchor pads 110a and 110 b and the relatively rigid retainer 200. For example, the basemembers 130 a and 130 b may help secure the retainer 200 to the anchorpads 110 a and 110 b and stabilize the retainer 200 so as to betterwithstand twisting about the lateral axis.

With reference now to the retainer 200, it can be seen in FIG. 1 thatthe retainer 200 comprises an open channel 234, a strap 240, and twoangled supports 250 and 255. The retainer 200 is attached to andsupported by the base members 130 a and 130 b and is configured suchthat the retainer 200 does not rock or otherwise pivot on the basemembers 130 a and 130 b. In some embodiments, the retainer 200 ispermanently adhered or affixed to the base members 130 a and 130 b.

The open channel 234 has a curvilinear shape configured to accept atleast a portion of a medical article. In the illustrated embodiment, theopen channel 234 is configured to accept a catheter hub and thus theshape of the channel 234 approximates at least a portion of the catheterhub. The channel 234 is shown as having an approximately semi-conicalshape, but may be formed as having a different shape. In the illustratedembodiment, the width of the channel 234 in the lateral direction variesin width such that a portion of the channel tapers in a direction fromdistal to proximal, but the channel 234 may be a consistent width ortapered along the entire channel. As will be described below, thechannel 234 may be configured to accept various medical articles.

A strap 240 is attached to the first angled support 255. The strap 240is configured to close over the open channel 234 and onto the secondangled support 250 to form an enclosed area. When at least a portion ofa medical article is placed inside the channel 234, the strap 240 can bemoved over the medical article to retain or stabilize the medicalarticle within the retainer 200 by, for example, applying a downwardforce onto the medical article and thus maintaining at least a portionof the medical article on a surface of the channel 234. The strap 240may be integral to the first angled support 255, or may be attachedthereto. In one embodiment, the strap 240 is integral to the firstangled support 255 and attached by a living hinge. In anotherembodiment, the strap 240 is formed separate from the first angledsupport 255 and attached thereto, for example by sonic welding. Amultitude of attachment means may be used to attach the strap 240 to thefirst angled support 255 such that the strap 240 may be closed over thechannel 234 and onto the second angled support 250.

As illustrated in FIG. 1, the strap 240 is attached to the first angledsupport 255 by a pin 242 that passes through the first angled support255 and the strap 240. As such, the strap 240 can rotate about the pin242 to cover and uncover the channel 234. The first angled support 255includes grooves 258 a and 258 b for receiving a portion of the strap240 when the strap 240 is in a closed position.

In one embodiment, the strap 240 comprises an elastomeric material. Inthis embodiment, the strap 240 may be stretched or deformed slightlywhen closing about a medical article placed in the channel 234. That isto say, the strap 240 may conform to the outer surface of a medicalarticle placed within the channel 234 thus increasing the contact areabetween the medical article and the strap 240. Such elastic deformationmay increase the stability with which the medical article is securedwithin the channel 234. In addition, the elastomeric material may havean increased frictional coefficient with the medical article as comparedto certain other materials like hard plastics. In some embodiments, thestrap 240 may also have ribs or other protrusions formed on an insidesurface thereof. In this way, the ribs can further increase thefrictional coefficient with the medical article to further secure themedical article within the retainer 200.

In the illustrated embodiment, the strap 240 is formed with an opening244 therethrough. The opening 244 is configured to accept a retentionmechanism 239. The retention mechanism 239 is disposed on the secondangled support 250 in the illustrated embodiment. The second angledsupport 250 holds the retention mechanism 239 in a position such that itcan engage with the strap 240. The second angled support 250 may alsoserve to support, strengthen, or stabilize a portion of the channel 234.In some embodiments, the second angled support 250 is omitted. In thiscase, the retention mechanism 239 may be disposed on an outer surface ofthe channel 234 or on the base member 130 a.

In FIG. 1, a first securement mechanism, e.g., the retention mechanism239, is illustrated as being a protrusion disposed on the second angledsupport 250 that can be inserted through the opening 244 to retain thestrap 240 in a closed position over the channel 234. The retentionmechanism 239 may comprise a lip to overhang a portion of the strap 240after the retention mechanism 239 has been inserted through the opening244. Other securing means may be used in place of the illustratedretention mechanism 239. For example, the strap 240 may be secured abouta medical article by a snap, adhesive, hook and loop fasteners, or othersecuring means.

With continued reference to FIG. 1, a tab 246 extends away from theportion of the strap 240 and has the opening 244. The tab 246 may beformed of the same or different material as the strap 240. The tab 246may include ridges, bumps, or other raised features to distinguish thetab 246 from the strap 240. The tab 246 may allow a medical provider toeasily grip the strap 240 and to engage and/or disengage the strap 240from the retention mechanism 239. In some embodiments, the tab 246 has athickness less than the strap 240 and/or may be configured to move aboutthe end of the strap 240. In some embodiments, the tab 246 is omitted.

In the illustrated embodiment, the second angled support 250 comprises asecond securement mechanism, e.g., protrusions 252 a and 252 b alongeach edge of the second angled support 250. As shown, the protrusions252 a and 252 b are integrally formed with the second angled support 250and run along the entire length of the second angled support 250 forminga channel that can receive a portion of the strap 240. The protrusions252 a and 252 b can limit movement of the strap in the longitudinaldirection when the strap 240 is secured over the channel and onto thesecond angled support 250. In some embodiments, the protrusions 252 aand 252 b are formed separately and are attached to the second angledsupport 250. In some embodiments, the protrusions 252 a and 252 b do notcover the entire length of the second angled support 250. In someembodiments, the second angled support 250 includes a single protrusionalong one edge of the second angled support 250.

The retainer 200 may be constructed as a single piece or from aplurality of different pieces. For example, the entire retainer 200 maybe formed by injection molding, or the channel 234 and the angledsupports 250 and 255 may be formed separately and thereafter joinedtogether. The retainer 200 or portions thereof may be rigid or flexible.Suitable materials may include, for example, but without limitation,plastics, polymers or composites such as polypropylene, polyethylene,polycarbonate, polyvinylchloride, acrylonitrile butadiene styrene,nylon, olefin, acrylic, polyester, as well as moldable silicon,thermoplastic urethane, thermoplastic elastomers, thermoset plastics andthe like. In one embodiment, the retainer 200 is formed by injectionmolding using a polyethylene or a polypropylene material or nylon.However, other materials can be utilized.

FIG. 2 is a top view of the retainer 200 shown in FIG. 1. From above,the geometry of the channel 234 of one embodiment of the retainer 200can be appreciated. The channel 234 may comprise a distal portion 233and a proximal portion 232. As shown, the width of the distal portion233 is greater than the width of the proximal portion 232. In this way,the channel 234 can be sized and shaped such that a complementary shapedmedical article can fit snuggly within the channel 234. In other words,the particular dimensions of the channel 234 can be adjusted such thatthe contact area between the medical article and the channel 234 ismaximized.

FIG. 3A is a cross-sectional view of the retainer 200 in FIG. 2 takenalong the line 3A-3C. This cross-sectional view further exemplifies thegeometry of the channel 234 of one embodiment of the retainer 200. Asshown, the interior of the channel 234 includes a lower abutment surface231 and an upper abutment surface 229. The lower and upper abutmentsurfaces 231 and 229 can prevent a suitably shaped medical article frommoving in at least a proximal direction. The channel 234 also includesan upper abutment 236 on the exterior of the channel. The upper exteriorabutment 236 can contact a portion of a medical article placed withinthe channel 234. For example, the upper exterior abutment 236 cancontact a proximal surface of a catheter fitting attached to a catheterhub positioned within the channel 234, as will be described in greaterdetail below, so as to prevent movement of the catheter fitting in theproximal direction. Similarly, the upper exterior abutment 236 cancontact a surface of a catheter hub positioned within the channel 234.For example, the upper exterior abutment 236 can contact a proximalsurface of a male luer-lock portion of a catheter hub positioned withinthe channel 234.

FIG. 3B is a cross-sectional view of a retainer 200 in FIG. 2 takenalong the line 3A-3C according to another embodiment. As illustrated,the channel 234 b in this embodiment does not include interior abutmentsurfaces. Furthermore, the width of the channel 234 b is uniform. Thechannel 234 b also includes an upper exterior abutment 236 and a lowerexterior abutment 238. The upper exterior abutment 236 and/or lowerexterior abutment 238 can contact a portion of a medical article placedwithin the channel 234 b as described above. The inclination angle θ ofthe channel 234 b with respect to the transverse direction may be anysuitable angle. In some embodiments the inclination angle θ is betweenabout 5 and about 10 degrees, for example, about 7 degrees, relative tothe patient's skin.

FIG. 3C is a cross-sectional view of a retainer 200 in FIG. 2 takenalong the line 3A-3C according to another embodiment. As shown, in thisembodiment, the width of the channel 234 c is not uniform. Rather, thewidth of the distal portion 233 c of the channel 234 c is greater thanthe width of the proximal portion 232 c of the channel 234 c. In thisway, the channel 234 c can be shaped to receive, for example, aconically shaped medical article. Such a conically shaped medicalarticle, positioned within the channel 234 c, can abut the surface ofthe channel 234 c and thus can be prevented from moving in the proximaldirection.

FIG. 4 is a front view taken from the proximal end of a retainer 200 ofFIG. 1 according to one embodiment. From this view, the shape of thechannel 234 can be further appreciated. As shown, the channel 234 isshaped roughly as an inclined tapered cylindrical section. FIG. 4illustrates that the channel 234 is slightly angled such that a distalportion of the channel slopes downward toward a proximal portion of thechannel. In this way, a medical article placed within the channel 234can be retained within the channel 234 and supported at a desiredinsertion angle with respect to the transverse axis. The channel 234also narrows in width from the distal portion towards the proximalportion. As such, the channel 234 is shaped to receive a roughlyconically shaped medical article that tapers in the proximal direction.

FIG. 4 also illustrates that the first angled support member 255 slopesdownward from a distal portion of the first angled support member 255towards a proximal portion of the first angled support member 255. Insome embodiments, the angle of inclination of the first angled support255 in the longitudinal direction is roughly the same as a roughlyconically shaped medical article, tapered in the proximal direction.That is to say, the first angled support member 255 can be shaped suchthat a complementary shaped medical article can fit snuggly against thefirst angled support member 255. This configuration can allow the strap240 to contact a greater area on the upper surface of the first angledsupport member 255 when the strap 240 is closed over the channel 234.

Continuing with FIG. 4, the strap 240 comprises a first strap section241 and a second strap section 249. When the strap 240 is positionedover the channel 234, the first strap section 241 can contact the firstangled support member 255 and a medical article positioned within thechannel 234 while the second strap section 249 can contact the secondangled support member 250 and engage the retention mechanism 239. Thefirst strap section 241 and second strap sections 249 can comprise thesame material as each other or be formed of different materials. Forexample, the first strap section 241 can comprise a rigid material whilethe second strap section 249 can comprise an elastomeric material. Thefirst strap section 241 and second strap sections 249 can be formed asone integral strap joined by a hinge 245 (for example, a living hinge)or formed separately and coupled together.

As shown in FIG. 4, the first strap section 241 has a lower surfaceshaped to receive a portion of a medical article. The first strapsection 241 generally increases in thickness in a direction away fromthe first angled support member 255 and includes an indentation 248. Thesecond strap section 249 has a thickness less than the thickness of thefirst strap section 241. However, the relative thicknesses of the firstand second strap sections 241 and 249 can be the same and the secondstrap section 249 can have thickness greater than the thickness of thefirst strap section 241. The indentation 248 can be shaped to receive atleast a portion of an upper surface of a medical article, for example,the upper surfaces of a catheter hub. In one embodiment the indentation248 is curvilinearly shaped. In this way, the strap 240 can be sized andshaped such that a complementary shaped medical article can fit snugglyagainst the strap 240. In other words, the particular dimensions of thestrap 240 can be adjusted such that the contact area between the medicalarticle and the strap 240 is maximized.

FIG. 5 is a rear view taken from the distal end of the retainer 200 ofFIG. 4. From this view, one can further appreciate the geometry of thechannel 434 according to the illustrated embodiment. As shown, thechannel 234 is crescent shaped and greater than semi-circular whenviewed from the distal end of the securement device 100. As such, thechannel 234 can receive a medical article inserted from both thetransverse and/or longitudinal directions while at the same time thecontact area between the channel 234 and the exterior surface of themedical article placed therein can be maximized. In some embodiments,the channel 424 does not have generally rounded sides. For example, thesides of the channel 234 may be angled in relation to themselves or inrelation to each other to accommodate a differently shaped medicalarticle.

FIG. 6 illustrates the securement device 100 in FIG. 1 with a medicalarticle positioned above. As shown, a catheter 610 is attached to acatheter hub 630. In some embodiments, the catheter 610 or a portionthereof comprises or is coated with an antimicrobial agent and/or anantibacterial agent. The antimicrobial agent may comprise a silvermaterial, for example a silver salt, colloid, or complex. In oneembodiment, one or more oligodynamic metal salts, oxides, or combinationof salts and oxides are used.

FIG. 6 shows that anchor pad 110 a can extend a length L in the proximaldirection away from the retainer 200. This length L can serve asattachment surface for the dressing 120. In this way, the dressing 120can be positioned in an open position, away from the insertion site toallow easy access to the insertion site for a medical article. After themedical article is inserted into the patient, the dressing 120 can befolded over the length L to further protect the insertion area andsecure the medical article to the patient.

Catheter hubs are generally known to those skilled in the art. Thecatheter hub 630 shown in FIG. 6 has a proximal body 632, a conicalsection 636, and a distal body 612. However, different catheter hubs mayinclude more or less bodily sections of various different shapes andsizes, all of which may be used with the retainer 200 or otherembodiments of the retainers described herein. In one embodiment, thecatheter hub 630 comprises an integral one-way valve. The catheter hub630 is connected to an extension set 620. The extension set 620illustrated in FIG. 6 includes a spin nut 644 connected to a tube 622.The channel 234 is shaped to receive the catheter hub 630. For example,the proximal portion of the channel 232 is shaped to receive theproximal body 632 and the distal portion of the channel 233 is shaped toreceive the distal body 612.

Turning to FIG. 7, the catheter hub 630 may be placed within the openretainer 200 from above. With brief reference to FIG. 3B, one canappreciate that the conical section 636 may contact the lower and upperabutment surfaces 231 and 229 within the channel 234. As such, thecatheter hub 630 is prevented from moving in a proximal direction by atleast one abutment surface.

Moving on to FIG. 8, the securement device 100 is illustrated as securedto a hand 830 of a patient. Those of skill in the art, however, willrecognize that the securement device 100 may instead be secured to otherportions of a patient's body. Those of skill in the art will understandthat the relative positioning of various elements of the securementdevice 100 thus may be altered without compromising the advantagesprovided by the securement device 100. In some embodiments, thesecurement device 100 is configured as a mirror image of the deviceshown in FIG. 8.

Continuing with FIG. 8, the anchor pads 110 a and 110 b comprise distaltriangular sections 820 a and 820 b with rounded corners and proximalrectangular sections 830 a and 830 b with rounded corners. The proximalrectangular sections 830 a and 830 b support the base members 130 a and130 b and retainer 200 while the distal triangular sections 820 a and820 b further attach the securement device 100 to the left hand 800. Forexample, the lower surface of the distal triangular sections 820 a and820 b can adhere to an area proximal to the knuckles of the hand.However, other shapes and configurations of the anchor pads 110 a and110 b are possible and within the scope of this description. Forexample, the anchor pads 110 a and 110 b, may be larger or smaller, andmay be shaped for placement on a different area of the patient's body.In short, the anchor pads 110 a and 110 b may be any size or shape thatallows attachment of the anchor pads 110 a and 110 b to a patient's skinand that is configured to support at least the retainer 200.

In the illustrated embodiment, the strap 240 is configured to retain thecatheter hub 630. Thus, the strap 240 is sized and shaped such that itcan be placed over the portion of the catheter hub 630 that is exposedafter the catheter hub 630 has been placed in the channel. When thestrap 240 is formed of an elastomeric material, as described above, thestrap 240 may conform to the shape of the catheter hub 630 or otherretained medical article when pulled over the medical article or portionthereof. In the illustrated embodiment, the strap 240 does not securethe spin nut 644. That is to say, when the strap 240 is closed over thecatheter hub 630, the spin nut 644 can be rotated to release theextension set 620 from the catheter hub 630 while the catheter hub 630remains secured to the patient.

The catheter 610 can be inserted into the hand 800 and the catheter hub630 can be connected to the extension set 620 by using the spin nut 644before or after the catheter hub 630 is placed in the channel of theretainer 200. The anchor pads 110 a and 110 b may have already beenadhered to the hand 800, or the anchor pads 110 a and 110 b maythereafter be adhered to the hand 800. During this time, the dressing120 is held away from the catheter 610 and the insertion site. Thepositioning of the dressing 120 may be maintained by a medical provider,or the dressing 120 or the area of attachment of the dressing 120 toanchor pad 110 b may be configured so as to bias the dressing 120 inthis position.

The strap 240 is then pulled over the catheter hub 630 until the opening244 engages the retention mechanism 239. The retention mechanism 239will maintain the strap 240 in a closed position over the catheter hub630. At this time, the release liner 122 of the dressing is removed toexpose the adhesive surface 124. The dressing 120 is folded down overthe insertion site and adhered to the skin of the patient, as shown inFIG. 8. Of course, the dressing 120 may be adhered to the patient beforethe strap 240 is closed over catheter hub 630 and secured by theretention mechanism 239. To remove the catheter hub 630 from theretainer 200, the medical provider may use the tab 246 to release thestrap 240.

In this way, the catheter 610, catheter hub 630, and extension set 620may be stabilized by the securement device 100. In addition, theinsertion site of the catheter will be protected and preserved in asanitary fashion while the catheter is administered. The medicalprovider can ensure such protection at the time of stabilization of thecatheter, and need not leave the inserted catheter unattended to seek aform of protective covering for the insertion site.

Turning to FIG. 9, a cross-sectional view taken along the line 9-9 ofthe retainer 200 of FIG. 8 is illustrated. As shown, the strap 240 isclosed over the channel and secured by retention mechanism 239. In theclosed position, the lower surface of the strap 240 contacts at least aportion of first angled support 255, at least a portion of the catheterhub 630 positioned in the channel of the retainer 200, and at least aportion of the second angled support 255. The indentation 248 in thefirst strap section 241 can be shaped to accept the upper surface of acatheter hub 630 placed within the channel. The first strap section 241contacts less than the total surface area of the first angled support255 such that a gap 900 exists between the first strap section 241 andthe first angled support 255. The gap 900 may ensure that the entireunderside of the strap 240 above the catheter hub 630 contacts thecatheter hub 630. However, the gap 900 is not required, and the strap240 and/or the first angled support 255 can be shaped such that no gap900 is present when the strap 240 is closed over a medical articleplaced within the retainer 200.

The first strap section 241 can also contact a portion of the secondangled support 255. FIG. 9 also shows the relative heights h₁ and h₂ ofthe first and second angled supports 255 and 250 above the top surfacesof the base members 130 a and 130 b. As shown, the height of the firstangled support h₁ is greater than the height of the second angledsupport h₂.

FIG. 9 A shows a partial top view of the securement device of FIG. 8with the strap removed. As shown, the second angled support 255comprises two channels 258 a and 258 b. The channels 258 a and 258 b canserve as receiving spaces for at least a portion of the strap 240. Thestrap can be shaped such that a portion of the strap can fit within thechannels 258 a and 258 b. The strap can also include a bore through theend of the strap to be attached to the second angled support 255. Thebore can be configured to receive a pin. The second angled support 255can also include bores 259 for receiving a pin therethrough. In otherwords, a pin can pass through the second angled support 255 and thestrap in order to movably attach the strap to the retainer.

FIG. 10 illustrates a catheter assembly 700 that can be used with someembodiments of the securement device described herein. In someembodiments, the securement device is configured to retain the catheterassembly 700. The catheter assembly 700 can be an ADVANTIV® safety I.V.catheter available from Smiths Medical (Dublin, Ohio) or a similarcatheter. As shown, the catheter assembly 700 comprises an introducerneedle 705, a catheter 710, a catheter hub 730, a tip protector 740, anda flash chamber assembly 750. The catheter hub 730 has a proximal body731 and a distal body 739. The distal body 739 has an abutment surface735 and a male luer-lock connector 738. The abutment surface 735 cancontact at least a portion of a retainer to prevent the catheter hub 730from moving in at least a proximal direction. The male luer-lockconnector 738 can be used to connect the catheter hub 730 to a catheterextension set.

FIG. 11 illustrates an exploded view of the catheter assembly 700 ofFIG. 10. As shown, the tip protector 740 encloses the sharp proximal endof the introducer needle 705 and includes a tab 745. A medical providermay apply a force to a distal surface of the tab 745 while pulling onthe flash chamber assembly 750 to remove the flash chamber assembly 750,introducer needle 705, and tip protector 740 from the catheter hub 730.When the introducer needle 705 is moved distally, away from the catheterhub 730, the sharp proximal end of the introducer needle 705 engageswith the tip protector 740 such that the tip protector 740 encloses theproximal tip portion of the introducer needle 705. In this way, thesharp tip of the introducer needle 705 is shielded, for example, toreduce the likelihood of accidental needle pricks.

FIGS. 12-17 illustrate a method of using the catheter assembly 700 andthe securement device 1600 shown in FIG. 16 in the context of starting aperipheral I.V. line. The discussion of this embodiment and this examplemethod of use are meant to augment the description of the inventionabove and both should be read together.

In starting a peripheral I.V. line, the medical provider begins bypositioning the catheter assembly 700 over the hand 1200 of a patient asshown in FIG. 12. The method continues in FIG. 13 by inserting theintroducer needle 705 into the vasculature of the hand 1200. Thecatheter 710 can follow the introducer needle 705 into the vasculatureas the introducer needle 705 is advanced proximally.

Turning to FIG. 14, the introducer needle 705 is removed by pulling onflash chamber assembly 750 and moving the flash chamber assembly 750 ina distal direction. The flash chamber assembly 750 separates from thetip protector 740 under a sufficient force in the distal direction. Theintroducer needle 705 is coupled to the flash chamber assembly 750.Thus, as the flash chamber assembly 750 is withdrawn distally, theintroducer needle 705 is also withdrawn distally through the catheter710 and tip protector 740 as illustrated.

The method continues in FIG. 15 as the flash chamber assembly 750 ismoved further distally. As shown, when the proximal tip portion of theintroducer needle 705 is withdrawn into the tip protector 740, the tipprotector 740 engages the proximal tip portion of the introducer needle705. Thus, the proximal end of the introducer needle 705 becomes coupledto the tip protector 740. The tip protector 740 then separates from thecatheter hub 730 as the flash chamber assembly 750 is moved furtherdistally from the insertion site.

The medical provider can then attach a connector to the catheter hub 730to establish fluid communication between the catheter hub 730 and amedical line. The connector can be configured to attach to a medicalarticle for carrying fluids to or from the catheter 710, for example toa catheter extension set. The connector may therefore be formed with alumen extending therethrough along a generally longitudinal axis inorder to carry the fluids. In the illustrated embodiment, the connectoris configured with a female luer-lock connection fitting to accept themale luer-lock connection fitting 738 disposed on the catheter hub 730.In some embodiments, the connector comprises a vented one-way valve.

With reference now to FIG. 16, an embodiment of a securement device 1600includes anchor pads 1610 a and 1610 b, a dressing 1620, and a retainer1650. The anchor pads 1610 a and 1610 b and retainer 1650 may all beconfigured similar to the embodiments described above with respect toFIG. 1. The anchor pads 1610 a and 1610 b may also include releaseliners 1615 a and 1615 b similar to or the same as release liners 115 aand 115 b. The retainer 1650 may comprise materials similar to thosedescribed above with respect to the retainer 200. Similarly, theretainer 1650 may be formed as a single unit, or may be formed asseveral different elements and integrated together.

In the illustrated embodiment, the dressing 1620 is covered by a releaseliner 1621. The release liner 1621 may be configured similar to therelease liner 121 described with respect to FIG. 1. The dressing 1620has an adhesive surface 1624 and an occlusive layer 1626. The adhesivesurface 1624 and occlusive layer 1626 can be configured similar to theadhesive surface 124 described with respect to FIG. 1. However, incontrast to the adhesive surface 124 described with respect to FIG. 1,the adhesive surface 1624 of the dressing 1620 is not disposed over thesurface of an occlusive layer 1626 of the dressing 1620. Of course, theadhesive surface 1624 may instead be disposed over the entire surface ofthe occlusive layer 1626 of the dressing 1620, for example in any of theways described above with respect to the adhesive surface 124 and theocclusive layer 126. The release liner 1621 covers the adhesive surface1624 and can be removed prior to applying the adhesive surface to, forexample, the skin of a patient. As shown, similar to FIG. 1, theadhesive surface 1624 and release liner 1621 do not cover an edge 1622of the dressing to form a tab as described above.

The dressing 1620 may otherwise be configured similar to the dressing120 described with respect to FIG. 1. However, the attachment of thedressing 1620 to the anchor pad 110 a may be configured differently thanthe attachment of the dressing 120 to the anchor pad 110 a. In FIG. 16,the dressing 1620 of the securement device 1600 is attached to the rearportion of anchor pad 110 b by a flap 1625. The flap 1625 can comprisethe same or similar materials as the anchor pad 110 a and/or occlusivelayer 1626. The dressing 1620 can fold over the flap 1625 as thedressing 1620 is rotated about the flap 1625 towards the distaldirection.

The method of using the securement device 1600 is shown as completed inFIG. 17. The catheter hub 730 is coupled to extension set 620 byscrewing the spin nut 644 onto the catheter hub 730 before or after thesecurement device 1600 is attached to the hand and before or after thecatheter hub 730 is secured and stabilized by the retainer 1650. Thesecurement device 1600 is attached to the hand by removing the releaseliners 1615 a and 1615 b from the anchor pads 1610 a and 1610 b toexpose the lower adhesive surface of the anchor pads 1610 a and 1610 b,and placing the anchor pads 1610 a and 1610 b on the hand. The catheterhub 730 secured by the retainer by positioning at least a portion of thecatheter hub 730 into the channel of the retainer 1650, closing thestrap over the channel, and securing the strap with the retentionmechanism as discussed above.

The release liner 1624 of the dressing 1620 may be removed to expose theadhesive surface. The dressing 1620 is folded down over the insertionsite and adhered to the skin of the patient, as shown in FIG. 17. Atthis point, the catheter 610, catheter hub 730, and tube 622, are allsecured to the securement device 1600, and are stabilized on thepatient. The medical provider may then introduce fluids or medicamentsinto the catheter 610 for administration to the patient.

It is to be noted that the figures provided herein are not drawn to anyparticular proportion or scale, and that many variations can be made tothe illustrated embodiments. Those of skill in the art will recognizethat the disclosed aspects and features shown herein are not limited toany particular embodiment of a stabilization system, and stabilizationsystems that include one or more of the features herein described can bedesigned for use with a variety of medical articles.

The various embodiments of the stabilization systems described above inaccordance with the present invention thus provide a means to releasablysecure a connector fitting or extension set to a patient. An insertionsite of a catheter attached to the connector fitting or extension setmay be covered with an integrated dressing.

Of course, it is to be understood that not necessarily all objects oradvantages may be achieved in accordance with any particular embodimentof the invention. Thus, for example, those skilled in the art willrecognize that the invention may be embodied or carried out in a mannerthat achieves or optimizes one advantage or group of advantages astaught herein without necessarily achieving other objects or advantagesas may be taught or suggested herein.

Furthermore, the skilled artisan will recognize the interchangeabilityof various features from different embodiments. In addition to thevariations described herein, other known equivalents for each featurecan be mixed and matched by one of ordinary skill in this art toconstruct stabilization systems and techniques in accordance withprinciples of the present invention.

Although this invention has been disclosed in the context of certainembodiments and examples, it will be understood by those skilled in theart that the present invention extends beyond the specifically disclosedembodiments to other alternative embodiments and/or uses of theinvention and obvious modifications and equivalents thereof. Thus, it isintended that the scope of the present invention herein disclosed shouldnot be limited by the particular disclosed embodiments described above.

What is claimed is:
 1. A securement device for securing a catheter,comprising: a first anchor pad and a second anchor pad, wherein a gapseparates an edge of the first anchor pad from an adjacent edge of thesecond anchor pad; a retainer comprising: a first base member secured toan upper surface of the first anchor pad; a second base member securedto an upper surface of the second anchor pad; and a body coupled to thefirst base member and the second base member, wherein a portion of thebody spans the gap separating the first anchor pad from the secondanchor pad, the portion of the body including an open channel through anupper surface of the body, the open channel aligned with the gap, thebody comprising a first securement mechanism and a second securementmechanism; and a strap having a first end rotatably coupled to the bodyto transition the strap between an open position and a closed position,wherein in the closed position: the strap covers the open channel, and asecond end of the strap opposite of the first end engages both the firstsecurement mechanism and the second securement mechanism.
 2. Thesecurement device according to claim 1, further comprising a dressingattached to the first anchor pad, the dressing configured to moveindependently of the strap between an open configuration and a closedconfiguration.
 3. The securement device according to claim 2, wherein aproximal end of the first anchor pad extends a first length proximal ofa proximal end of the second anchor pad, wherein the dressing isattached to the first anchor pad along the first length.
 4. Thesecurement device according to claim 3, wherein the dressing isconfigured to rotate or fold from an uncovered position to a coveredposition, and wherein the dressing is proximal of the body of theretainer in the covered position.
 5. The securement device according toclaim 4, wherein the dressing is attached to the first length along ascore line.
 6. The securement device according to claim 2, wherein aportion of the dressing includes an adhesive surface, and wherein arelease liner covers the adhesive surface.
 7. The securement deviceaccording to claim 6, wherein the release liner includes a coatingselected from the group consisting of an anti-microbial, ananti-bacterial, an anti-hemorrhagic agent, and combinations thereof. 8.The securement device according to claim 1, wherein the first securementmechanism is a locking tab extending from a surface of the body, whereinthe second end of the strap includes an opening, and wherein the lockingtab passes through the opening in the closed position of the strap. 9.The securement device according to claim 8, wherein: the secondsecurement mechanism comprises continuous protrusions on opposing edgesof the body, the second end of the strap has a width less than adistance between the opposing edges of the body, the locking tab ispositioned between the opposing edges of the body, and the second end ofthe strap is positioned between the continuous protrusions in the closedposition of the strap.
 10. The securement device according to claim 1,wherein the body of the retainer comprises a first angled support and asecond angled support separated by the open channel, wherein the firstangled support is coupled to the first base member and the second angledsupport is coupled to the second base member.
 11. The securement deviceaccording to claim 10, wherein: the first end of the strap is rotatablycoupled to the second angled support, the first securement mechanism isa locking tab extending from a surface of the first angled support, thesecond end of the strap includes an opening, and the locking tab passesthrough the opening in the closed position of the strap.
 12. Thesecurement device according to claim 11, wherein: the second securementmechanism comprises continuous protrusions on opposing edges of thefirst angled support, the second end of the strap has a width less thana distance between the opposing edges of the first angled support, thelocking tab is positioned between the opposing edges of the first angledsupport, and the second end of the strap is positioned between thecontinuous protrusions in the closed position of the strap.
 13. Thesecurement device according to claim 1, wherein the first base member,the second base member, and the body are a single integral piece. 14.The securement device according to claim 1, wherein the strap comprisesan elastomeric material that conforms to an outer surface of thecatheter in the closed position of the strap.
 15. The securement deviceaccording to claim 1, wherein the retainer includes an exterior abutmentsurface to prevent movement of the catheter in the open channel.
 16. Thesecurement device according to claim 15, wherein the exterior abutmentsurface comprises an upper abutment surface and a lower abutmentsurface.
 17. The securement device according to claim 1, wherein thestrap includes a first strap section and a second strap section, thesecond strap section having a thickness less than a thickness of thefirst strap section.
 18. The securement device according to claim 17,wherein the first strap section is attached to the second strap sectionvia a hinge.
 19. The securement device according to claim 18, whereinthe first strap section includes an indentation with a curvilinear shapeat the hinge.
 20. The securement device according to claim 1, whereinthe open channel narrows from a first width to a second width smallerthan the first width.